A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611084



Internal ID6997995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142865147..142866553hg38UCSC Ensembl
Innerchr6:142865174..142866527hg38UCSC Ensembl
Outerchr6:142865121..142866580hg38UCSC Ensembl
chr6:143186284..143187690hg19UCSC Ensembl
Innerchr6:143186311..143187664hg19UCSC Ensembl
Outerchr6:143186258..143187717hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg381407
hg191407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12574635, essv12574636, essv12574634
SamplesHG03057, HG03832, HG03437
Known GenesHIVEP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611084
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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